Acta Herpetologica 1(2): 131-134, 2006

Temperature variation in nests of Caiman crocodilus (Crocodylia: Alligatoridae) Armando H. Escobedo Galván Escuela de Ciencias Biológicas, Universidad Nacional, Heredia, Costa Rica. Present address: Julio Cervantes 561 Col. San Lorenzo Oriente C.P. 25060 Saltillo, Coahuila, México. E-mail: elchorvis@gmail. com Abstract. Caiman crocodilus is a widely distributed species in the Neotropics; however, studies of incubation temperatures in wildlife are uncommon. Incubation temperatures in four nests of Caiman crocodilus were measured with a digital thermometer, in the National Wildlife Refuge Caño Negro, Costa Rica. Average temperatures in these four nests (no. 1-4) were 32.13 + 0.92 °C (no. 1), 32.46 + 0.77 °C (no. 2), 33.60 + 0.95 °C (no. 3), and 31.78 + 2.30 °C (no. 4). Temperature variations recorded showed higher temperatures than those reported from other studies in Caño Negro. The temperatures registered in this study will lead to a higher proportion of males within the caiman population, reducing the number of future reproducing females and, therefore, in the population viability. Keywords: Caiman crocodilus, nest temperatures, Costa Rica.

Reptiles have a wide range of sex-determination systems, including genotypic and environmental sex determination. In crocodilians, sex is only determined by incubation temperature (Bull and Charnov, 1989; Thorbjarnarson, 1997), a kind of environmental sex determination. Most studies relating incubation with temperature have been carried out in laboratory conditions, because they permit knowledge of the sex ratios under different incubation temperatures (Aguilar-Miguel et al., 1998). However, these treatments do not necessarily encompass temperature variations that occur in the natural environment. Incubation temperature affects the sex ratio of crocodilian species differently. Studies of the effect of incubation temperature in crocodilians have been done with Alligator mississippiensis (Ferguson and Joanen, 1982), Caiman yacare (Campos, 1993; Miranda et al., 2002), C. latirostris (Piña et al., 2003), Crocodylus porosus (Magnusson, 1979), C. acutus and C. moreletii (Aguilar, 1995). Even though Caiman crocodilus is a widely distributed species in the Neotropics (Ross, 1998), studies of incubation temperatures in their natural environment are uncommon (Allsteadt, 1994). The most common treatment that has been done in situ in order to measure temperature variations within the nest used mercury thermometers inside the egg cavities. This method only registered temperatures during a limited period of time (hours along some days or weeks) (Magnusson et al., 1990; All-

132

Armando H. Escobedo Galván

steadt, 1994; Miranda et al., 2002; Casas-Andreu, 2003) and, it did not evaluate the thermal gradient present inside the egg cavities. Due to the lack of information about the variations of temperatures within C. crocodilus nests, the objective of this note is to analyze the daily variations of temperatures within nests of C. crocodilus located in the northern part of Costa Rica and compare our results with the others existing studies (Allsteadt, 1994; Junier, 2000). The study was conducted on the National Wildlife Refuge Caño Negro, on the Frio River, at the northern part of Costa Rica (10°54’N, 84°47’W). This protected area extends 9,969 ha and is one of the most important wetlands in northern of Costa Rica. Largest population density of C. crocodilus (74.36 ind/km) registered up to now has been reported at this location (Cabrera et al., 2003). The nests were located by walking transects in the sites where people had seen caiman nests in previous years. Caimans construct mounds of vegetation with leaves, grass, branches and earth in forested areas; mostly in the root area at the base of trees and near water bodies (Cintra, 1988; Álvarez del Toro and Sigler, 2001). When nest was discovered, it was opened to determine the presence of the eggs, because in some cases female caimans build up a nest without laying the eggs (Álvarez del Toro and Sigler, 2001). Once the eggs were observed at the egg cavity, a digital thermometer (StowAway TidbiT Temp Logger) was placed to register the temperature inside the egg cavity every 10 min, until the eggs hatched. The temperature was registered in four nests; no. 1, no. 2, no. 3 and no. 4 during 32, 31, 20 and, 69 days, respectively. The data were averaged daily, for interpretation. The Kruskal-Wallis test suggests differences between incubation temperature of the nests (H = 787.266; P < 0.01), with the highest mean temperature being in nest no. 3 (33.60 + 0.95 °C), followed by nest no. 2 (32.46 + 0.77 °C), nest no. 1 (32.13 + 0.92 °C) and nest no. 4 (31.78 + 2.30 °C) (Table 1). Only one nest (no. 3) indicates significant difference in temperatures between day and night, being higher during the night (Student t-test, P < 0.05). Temperature variations can be correlated with climatic phenomena. Magnusson (1979) observed that the presence of hurricanes affected the temperature within the nests. Location of the nests at the refuge can significantly alter temperatures. Cintra (1988) mentions that in some cases the nests are not placed at the best sites, because of intraspecific pressure or anthropogenic effects. Campos (1993) also observed that the nests that were built on top of organic matter showed higher temperatures than those that were built on top of floating grass. She concluded that nest temperature is determined by nesting habitat but that the effect of habitat depends on weather conditions.

Table 1. Incubation temperature of four nests with mean, standard deviation, minimum and maximum, registered with a digital thermometer in degrees Celsius. Nest



Mean

SD

Minimum

Maximum

no.1

757

32.13

0.92

25.57

33.39

no.2

735

32.46

0.76

29.11

33.73

no.3

468

33.60

0.95

29.73

35.03

no.4

1654

31.78

2.30

24.82

38.01

Temperature variation in nests of Caiman crocodilus

133

Allsteadt (1994) and Junier (2000) registered a mean of 31.8 °C and 31.6 °C, respectively in C. crocodilus nests in Caño Negro. Even though, there was not a statiscally significant difference between those studies and this research (Chi-square test, P > 0.05); there is an increase, in average, of 0.53 °C in incubation temperatures. Sometimes crocodilian females built nests on top of old nests, which allows for higher temperatures and also insulates the eggs from low ground temperatures (Magnusson et al., 1990). This fact could explain the higher recorded temperatures at the nests in this research. Temperature variations registered showed higher variations than those reported in other studies of crocodilians (Chabreck, 1973; Magnusson, 1979; Magnusson et al., 1985; Campos, 1993; Allsteadt, 1994). The higher temperatures of the nests implicate less reproductive success and decreased numbers of developed embryos but at the same time, hatchlings can be favored by a better growth in length and by a better increase in weight (Piña et al., 1997). Miranda et al. (2001) observed that hatchlings of caiman nests of temperatures higher than 31 °C presented a better absorption of the yolk and, a faster feeding after hatching. In nest no. 1 there were five post-hatching dead newborns, and no eggs hatched from nest no. 4. We suggest that phenomenon is due to the high and low temperatures registered at those nests, in accordance with the observations of Ferguson and Joanen (1982). Campos (1993) determined that temperatures higher than 31.5 °C within the nest produce a higher number of males. Assuming that the critical temperature for the production of clutches with 1:1 sex ratios is about 31.5 °C, the proportion of sexes in the observed nests could be higher than 75% male. This could have repercussions on the number of future reproducing females and, therefore, in the viability of the population.

ACKNOWLEDGEMENTS This study was supported by Roberto Villalobos and José Retana who work at the Instituto Meteorológico Nacional of Costa Rica. I thank the staff of National Wildlife Refuge Caño Negro. I thank Marco A.L. Zuffi and the reviewers, whose comments helped to improve this note.

REFERENCES

Aguilar, X. (1995): Efecto de la temperatura de incubación sobre la determinación del sexo en Crocodylus acutus y C. moreletii. Bol. Soc. Herpetol. Mex. 6: 43. Aguilar-Miguel, X., Herrera, J., Merchant-Larios, H., Casas-Andreu, G. (1998): Efecto de la temperatura de incubación sobre la actividad esteroidogénica en Crocodylus acutus y C. moreletii. Rev. Soc. Mex. Hist. Nat. 48: 95-103. Allsteadt, J. (1994): Nesting ecology of Caiman crocodilus in Caño Negro, Costa Rica. J. Herpetol. 28: 12-19. Álvarez del Toro, M., Sigler, L. (2001): Los Crocodylia de México. 1a Edición. IMERNAR, PROFEPA, México. Bull, J.J., Charnov, E.L. (1989): Enigmatic reptilian sex ratios. Evolution 43: 1561-1566.

134

Armando H. Escobedo Galván

Cabrera, J., Protti, M., Urriola, M., Cubero, R. (2003): Distribución y abundancia de Caiman crocodilus en el Refugio Nacional de Vida Silvestre Caño Negro, Costa Rica. Rev. Biol. Trop. 51: 571-578. Campos, Z. (1993): Effect of habitat on survival of eggs and sex ratio of hatchlings of Caiman crocodilus yacare in the Pantanal, Brazil. J. Herpetol. 27: 127-132. Casas-Andreu, G. (2003): Ecología de la anidación de Crocodylus acutus (Reptilia: Crocodylidae) en la desembocadura del río Cuitzmala, Jalisco, México. Acta Zool. Mex. (n.s.) 89: 111-128. Chabreck, R.H. (1973): Temperature variation in nests of the American Alligator. Herpetologica 29: 48-50. Cintra, R. (1988): Nesting ecology of the Paraguayan Caiman (Caiman yacare) in the Brazilian Pantanal. J. Herpetol. 22: 219-222. Ferguson, M.W.J., Joanen, T. (1982): Temperature of egg incubation determines sex in Alligator mississippiensis. Nature 296: 850-853. Junier, E.F. (2000): Análisis de la población de Caiman crocodilus en el Refugio Nacional de Vida Silvestre Caño Negro, Costa Rica. Unpublished degree thesis/Tesis de licenciatura. Universidad Nacional, Heredia, Costa Rica. Magnusson, W.E. (1979): Maintenance of temperature of crocodile nests (Reptilia, Crocodilidae). J. Herpetol. 13: 439-443. Magnusson, W.E., Lima, A.P., Hero, J.M., Sanaiotti, T.M., Yamakoshi, M. (1990): Paleosuchus trigonatus nests: sources of heat and embryo sex ratios. J. Herpetol. 24: 397400. Magnusson, W.E., Lima, A.P., Sampaio, R.M. (1985): Sources of heat for nests of Paleosuchus trigonatus and a review of Crocodilian nest temperature. J. Herpetol. 19: 199207. Miranda, M.P., De Moraes, G.V., Matines, E.N., Pinto, L.C., Barbosa, O.R. (2002): Thermic variation in incubation and development of Pantanal Caiman (Caiman crocodilus yacare) (Daudin, 1802) kept metabolic box. Braz. Archiv. Biol. Technol. 45: 333-342. Piña, C.I., Larriera, A., Cabrera, M.R. (2003): Effect of temperature on incubation period, sex ratio, hatching success and survivorship in Caiman latirostris (Crocodylia, Alligatoridae). J. Herpetol. 37: 199-202. Piña, C., Donayo, P., Barriera, A. (1997): Efecto de la temperatura de incubación de huevos de Caiman latirostris, sobre diversas variables reproductivas y de crianza, informe de avance. Memorias de las 4ta Reunión Regional del Grupo de Especialistas de Cocodrilos de América Latina y el Caribe 4: 137-143. Ross, J.P. (1998): Crocodiles. Status survey and conservation action plan, 2nd Edition. UICN/SSC. Crocodile Specialist Group. Gland, Switzerland and Cambridge, London. Thorbjarnarson, J. (1997): Are crocodilian sex ratios female biased? The data are equivocal. Copeia 1997: 451-455.

Temperature Variation in Nests of Caiman Crocodilus

Studies of the effect of incubation temperature in crocodilians have been done with Alligator mis- .... Status survey and conservation action plan, 2nd Edition.

70KB Sizes 2 Downloads 160 Views

Recommend Documents

Temperature-dependent geographic variation
59: 75–81. [in. Japanese with English summary]. Baba H, Hiyori Y, Kusaoke H. 2005. Geographic variation in the mitochondrial DNA of the. Genji-firefly Luciola cruciata in the Fossa Magna region, central Japan. Zenkoku Hotaru. Kenkyukai-shi (an annu

Mitochondrial DNA phylogeography of Caiman ...
Oct 1, 2008 - 3Laboratorio de Ana´lisis Espaciales, Instituto de Biologıa, Universidad Nacional ..... software Sequencer version 6.1 (Kessing, 2000), and a w2 ...

Mitochondrial DNA phylogeography of Caiman ...
Oct 1, 2008 - we utilized mitochondrial DNA (mtDNA) sequence data from 45 individuals of C. crocodilus ..... between parallel runs and by visualization of the .... Map of tropical America showing the traditionally accepted geographic ranges ...

hummingbird-nests-gfairy.pdf
Download. Connect more apps... Try one of the apps below to open or edit this item. hummingbird-nests-gfairy.pdf. hummingbird-nests-gfairy.pdf. Open. Extract.

Temperature modulation in ferrofluid convection
tude modulation prevail, i.e., when →0, a general solution .... describe the problem for the simplest case s=0 when N=1 and L=1 to obtain some analytic results.

Observation of time-invariant coherence in a room temperature ...
Oct 14, 2016 - placeable resource for quantum-enhanced technologies. However, decoherence effects .... theory [3, 26, 27, 37], the degree of quantum coherence in the state ρ of a quantum ..... and E. R. de Azevedo, NMR Quantum Information Processing

Measurement of Temperature and Reaction Species in ...
Cathode Diffusion Layer of a Free-Convection Fuel Cell. Tibor Fabian,a,z ... monitor spatial and temporal distributions of temperature and spe- cies within an .... reflects light in a narrow bandwidth determined by the total length of the grating ...

Effects of Temperature during Seed Development in ...
Among the factors affecting germinability of a seed lot are the environmental conditions under which the seeds are produced. The objective of this study was to determine the effects of temperature during seed development on seed quality of two Astera

ePub Fundamentals of Bias Temperature Instability in ...
This book discusses different ultra-fast characterization techniques for recovery artefact free BTI measurements. It also covers different direct measurements ...

Correlation Effects in Models of High Temperature ...
4.2 Circles indicate Q MC data for G ( π/ 2 , τ ) ; solid line is the e x act solution . ..... F or a full summary of these properties , w e refer the reader to the revie w ...

high-temperature superconductivity in water-treated graphite ...
Page 1 of 19. 1. The following article has been published in final form at: http://onlinelibrary.wiley.com/doi/10.1002/adma.201202219/abstract. Can doping graphite trigger room temperature superconductivity? Evidence for granular high-temperature sup

Unusual temperature dependence in dissociative ...
Jul 20, 2001 - [1·4]. Such data are of direct relevance in any .... room temperature) which ensures a constant .... By comparing with electron scattering data it.

Observation of time-invariant coherence in a room temperature ...
Oct 14, 2016 - ena and thermodynamics) or by a task for which coherence is required ... ρ t free induction decay. 1. 2J. Cl. Cl. 13C. 1H. Cl. A t. B. C. E. F. = 0.

Direct mapping of the temperature and velocity gradients in discs ...
(2017) recently intro- duced a method to map the thermal and density gas structure of ...... We use the Monte Carlo radiative transfer code MCFOST. (Pinte et al.

Measurement of Temperature and Reaction Species in ...
1550 nm broadband light source (HP 83437A, Hewlett-Packard), and an optical .... Comparison of relative humidity measurements by the microprobe used here ...

potential-of-supercritical-carbon-dioxide-cycle-in-high-temperature ...
Page 1 of 6. Supercritical CO2 Power Cycle Symposium. May 24-25, 2011. Boulder, Colorado. The Potential of the Supercritical Carbon Dioxide Cycle in High Temperature. Fuel Cell Hybrid Systems. Muñoz de Escalona, José M. Thermal Power Group, Univers

Temperature dependence of the training effect in ...
mental big advantage, the HL magnetization can be isother- mally tuned by a .... consistent with our training data, the SL magnetization rever- sal is broadened for a ... Figure 4 shows the detailed analysis, 0HB vs n, of the SL training loops at ...

Temperature compensated overdrive in vertically ...
Dec 29, 2008 - ... Department of Electronics and Information Systems, B-9000 Ghent, Belgium ... 16.67 ms, 60 Hz refresh rate) and in the static case are es-.

evolutionary significance of geographic variation in a ... - BioOne
3E-mail: [email protected]. 4Centre for Ecological Research, Polish Academy of Sciences, 05-092 Łomianki, Dziekanów Lesny, Poland. 5University of Arizona, Arizona Research Laboratories Division of Neurobiology, 611 Gould-Simpson Building, Tucson

Intrageneric variation in antipredator responses of coral ...
(2009) Physiological basis for high CO2 tolerance in marine ectothermic animals: pre-adaptation through lifestyle and ontogeny? Biogeosciences, 6, 2313–2331. Miller AW, Reynolds AC, Sobrino C, Riedel GF (2009) Shellfish face uncertain future in hig